FDA Regulatory Education for Industry (REdI) – Devices Track

Presenters in the devices track discuss the following topics: Demystifying Medical Device Regulations, Accelerating Medical Device Innovation, Q-Sub Program, 510K Program, Bioresearch Monitoring Sponsor Inspections, Postmarket, and CAPA.

For all conference recordings, visit https://www.fda.gov/drugs/regulatory-education-industry-redi-annual-conference-2021-07192021-07232021

Agenda: https://www.fda.gov/REdI2021

Upcoming Training https://www.fda.gov/cdersbia

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SBIA 2021 Playlist - https://youtube.com/playlist?list=PLey4Qe-UxcxYS1MaTusSgyifQDqdeepyD

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Видео FDA Regulatory Education for Industry (REdI) – Devices Track канала U.S. Food and Drug Administration